TY - JOUR
T1 - Human Cryptic Host Defence Peptide GVF27 Exhibits Anti-Infective Properties against Biofilm Forming Members of the
Burkholderia cepacia Complex.
AU - Bosso, Andrea
AU - Gaglione, Rosa
AU - Di Girolamo, Rocco
AU - Veldhuizen, Edwin J A
AU - García-Vello, Pilar
AU - Fusco, Salvatore
AU - Cafaro, Valeria
AU - Monticelli, Maria
AU - Culurciello, Rosanna
AU - Notomista, Eugenio
AU - Arciello, Angela
AU - Pizzo, Elio
N1 - Funding Information:
Funding: This study was supported by the Italian Cystic Fibrosis Foundation (grant numbers 16/2017 and 18/2018). We are deeply indebted to volunteers who devote many efforts in fundraising, in particular Gruppo di Sostegno FFC di San Giovanni Rotondo, Guadagnin srl, Delegazione FFC di Reggio Calabria, Delegazione FFC di Imola e Romagna.
Publisher Copyright:
© 2022 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2022/2/21
Y1 - 2022/2/21
N2 - Therapeutic solutions to counter Burkholderia cepacia complex (Bcc) bacteria are challenging due to their intrinsically high level of antibiotic resistance. Bcc organisms display a variety of potential virulence factors, have a distinct lipopolysaccharide naturally implicated in antimicrobial resistance. and are able to form biofilms, which may further protect them from both host defence peptides (HDPs) and antibiotics. Here, we report the promising anti-biofilm and immunomodulatory activities of human HDP GVF27 on two of the most clinically relevant Bcc members, Burkholderia multivorans and Burkholderia cenocepacia. The effects of synthetic and labelled GVF27 were tested on B. cenocepacia and B. multivorans biofilms, at three different stages of formation, by confocal laser scanning microscopy (CLSM). Assays on bacterial cultures and on human monocytes challenged with B. cenocepacia LPS were also performed. GVF27 exerts, at different stages of formation, anti-biofilm effects towards both Bcc strains, a significant propensity to function in combination with ciprofloxacin, a relevant affinity for LPSs isolated from B. cenocepacia as well as a good propensity to mitigate the release of pro-inflammatory cytokines in human cells pre-treated with the same endotoxin. Overall, all these findings contribute to the elucidation of the main features that a good therapeutic agent directed against these extremely leathery biofilm-forming bacteria should possess.
AB - Therapeutic solutions to counter Burkholderia cepacia complex (Bcc) bacteria are challenging due to their intrinsically high level of antibiotic resistance. Bcc organisms display a variety of potential virulence factors, have a distinct lipopolysaccharide naturally implicated in antimicrobial resistance. and are able to form biofilms, which may further protect them from both host defence peptides (HDPs) and antibiotics. Here, we report the promising anti-biofilm and immunomodulatory activities of human HDP GVF27 on two of the most clinically relevant Bcc members, Burkholderia multivorans and Burkholderia cenocepacia. The effects of synthetic and labelled GVF27 were tested on B. cenocepacia and B. multivorans biofilms, at three different stages of formation, by confocal laser scanning microscopy (CLSM). Assays on bacterial cultures and on human monocytes challenged with B. cenocepacia LPS were also performed. GVF27 exerts, at different stages of formation, anti-biofilm effects towards both Bcc strains, a significant propensity to function in combination with ciprofloxacin, a relevant affinity for LPSs isolated from B. cenocepacia as well as a good propensity to mitigate the release of pro-inflammatory cytokines in human cells pre-treated with the same endotoxin. Overall, all these findings contribute to the elucidation of the main features that a good therapeutic agent directed against these extremely leathery biofilm-forming bacteria should possess.
KW - Agglutinating activity
KW - Anti-biofilm agents
KW - Antimicrobial peptides
KW - Host defence peptides
KW - Immunomodulatory activities
KW - LPS neutralisation
KW - Synergy
UR - http://www.scopus.com/inward/record.url?scp=85125266657&partnerID=8YFLogxK
U2 - 10.3390/ph15020260
DO - 10.3390/ph15020260
M3 - Article
C2 - 35215373
SN - 1424-8247
VL - 15
SP - 1
EP - 21
JO - Pharmaceuticals (Basel, Switzerland)
JF - Pharmaceuticals (Basel, Switzerland)
IS - 2
M1 - 260
ER -